嗜中性粒细胞及其外排产物对生物膜生物量、细菌活力和大肠杆菌共轭转移的影响

I. Maslennikova, I. V. Nekrasova, Erjavec M. Starčič, M. Kuznetsova
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引用次数: 0

摘要

本研究的目的是探讨中性粒细胞及其抗菌因子--过氧化氢和防御素α--对生物膜生物量、生物膜中细菌存活率以及大肠杆菌 N4i pOX38:Cm 菌株的 pOX38:Cm 质粒共轭转移到不同大肠杆菌菌株(共生菌 К12 TG1 和泌尿致病菌 DL82、R32 和 R45)的影响。与对照组相比,当加入 10⁵ cells/ml 的中性粒细胞时,带有供体大肠杆菌 N4i pOX38:Cm 的受体大肠杆菌 TG1 的生物膜增加,而尿路致病性大肠杆菌受体菌株 DL82、R32 和 R45 的生物膜生物量增加。大肠杆菌受体菌株 DL82/E. coli R45 与供体大肠杆菌 N4i pOX38:Cm 分别在加入 10⁶/10⁴-10⁶ cells/ml 中性粒细胞时生物膜生物量减少。与对照组相比,当加入 10⁴、10⁵、10⁶ 个/毫升的中性粒细胞时,受体大肠杆菌 TG1 细胞和转染体在生物膜中的存活率更高。加入 0.1 mM H₂O₂ 会增加大肠杆菌 DL82 和大肠杆菌 R45 的生物膜形成,加入 0.5 mM H₂O₂ 会减少大肠杆菌 DL82 的生物膜形成,而 0.5 mM 或 2.5 mM 会减少共轭混合物中大肠杆菌 R45 的细菌生物膜生物量。与对照组相比,N4i pOX38:Cm × DL82 生物膜中存在 2.5 mM H₂O₂ 时,pOX38:Cm 共轭转移的频率较低,N4i pOX38:Cm × R45 生物膜中存在 0.5 和 2.5 mM H₂O₂ 时,pOX38:Cm 共轭转移的频率也较低。当加入 5 或 25 ng/ml defensin α 时,供体大肠杆菌 N4i pOX38:Cm 与大肠杆菌 DL82 的 pOX38:Cm 共轭频率降低;当加入 5 ng/ml defensin α 时,交配混合物 N4i pOX38:Cm×R45 的共轭频率降低,而当加入 25 ng/ml defensin α 时,共轭频率升高。
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The influence of neutrophils and their exoproducts on biofilm biomass, bacterial viability and conjugative transfer into Escherichia Coli
The purpose of this study was to investigate the effect of neutrophils and their antimicrobial factors, hydrogen peroxide and defensin α, on the biofilm biomass, the viability of bacteria in the biofilm and the efficiency of conjugative transfer of the pOX38:Cm plasmid from the E. coli N4i pOX38:Cm strain into different E. coli strains (commensal К12 TG1 and uropathogenic DL82, R32 and R45). The biofilm of the recipient E. coli TG1 with the donor E. coli N4i pOX38:Cm increased when 10⁵ cells/ml of neutrophils were added compared to the control, while the biofilm biomass of the uropathogenic E. coli recipient strains DL82/E. coli R45 with the donor E. coli N4i pOX38:Cm decreased when 10⁶/10⁴–10⁶ cells/ml of neutrophils were added, respectively. The survival of recipient E. coli TG1 cells and transconjugants in the biofilm was, compared to the control, higher when 10⁴, 10⁵, 10⁶ cells/ml of neutrophils were added. The addition of 0.1 mM H₂O₂ increased biofilm formation of E. coli DL82 and E. coli R45, and addition of 0.5 mM H₂O₂ reduced biofilm formation of E. coli DL82, while 0.5 mM or 2.5 mM reduced the E. coli R45 bacterial biofilm biomass in the conjugative mixture. The frequency of the pOX38:Cm conjugative transfer was lower in the presence of 2.5 mM H₂O₂ in the N4i pOX38:Cm × DL82 biofilm, and also in the presence of 0.5 and 2.5 mM H₂O₂ in the N4i pOX38:Cm × R45 biofilm, compared to the control. The frequency of pOX38:Cm conjugation from the donor E. coli N4i pOX38:Cm into E. coli DL82 decreased, when 5 or 25 ng/ml defensin α were added and the conjugation frequency in the mating mixture N4i pOX38:Cm×R45 decreased, when 5 ng/ml were added, while, when 25 ng/ml of defensin α were added it increased.
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